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CAS 92673-40-0

:

ethyl 7-amino[1,2,4]triazolo[1,5-a]pyrimidine-6-carboxylate

Description:
Ethyl 7-amino[1,2,4]triazolo[1,5-a]pyrimidine-6-carboxylate is a chemical compound characterized by its unique triazole and pyrimidine ring structures, which contribute to its biological activity. This compound features an ethyl ester functional group, enhancing its solubility and reactivity. The presence of the amino group at the 7-position of the triazole ring is significant for potential interactions with biological targets, making it of interest in medicinal chemistry. The carboxylate moiety at the 6-position can participate in various chemical reactions, including esterification and amidation, which are valuable in drug development. Its molecular structure suggests potential applications in pharmaceuticals, particularly in the development of agents targeting specific enzymes or receptors. Additionally, the compound's stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in its practical applications. Overall, ethyl 7-amino[1,2,4]triazolo[1,5-a]pyrimidine-6-carboxylate represents a versatile scaffold for further chemical modifications and biological evaluations.
Formula:C8H9N5O2
InChI:InChI=1/C8H9N5O2/c1-2-15-7(14)5-3-10-8-11-4-12-13(8)6(5)9/h3-4H,2,9H2,1H3
SMILES:CCOC(=O)c1cnc2ncnn2c1N
Synonyms:
  • [1,2,4]Triazolo[1,5-A]Pyrimidine-6-Carboxylic Acid, 7-Amino-, Ethyl Ester
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